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PMID: 6250573 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Electron paramagnetic resonance detectable states of cytochrome P-450cam.

Biochemistry ·Vol. 19 ·No. 15 ·1980-07-22 ·Pages 3590-9

Lipscomb JD

Abstract

Cytochrome P-450cam is a low-spin Fe3+hemoprotein (g = 2.45, 2.26, and 1.91) which is made 60% high spin (g = 7.85, 3.97, and 1.78) at 12 K by the addition of 1 mol of substrate per mol of enzyme. Low-temperature EPR spectra show that the low-spin fraction of substrate-bound P-450cam contains two magnetic species. The majority species has an unusual EPR spectrum (g = 2.42, 2.24, and 1.97) which connot be simulated by using the range of crystal field parameters known for other heme proteins. The minority species has the same g values as substrate-free enzyme. Both low-spin species show Curie law temperature dependence below 50 K and have similar saturation behavior. Above 50 K the g = 2.42, 2.24, and 1.97 species rapidly loses signal intensity. The distribution of low-spin species is pH dependent (apparent pKa = 6.2) with the g = 2.42, 2.24, and 1.97 magnetic species favored at high pH. The substrate binding stoichiometry and the equilibria observed in the low-spin fraction suggest that there are not multiple protein forms of cytochrome P-450cam. Putidaredoxin and other effector molecules which specifically catalyze hydroxylation convert either the high-spin or the g = 2.42, 2.24, and 1.97 low-spin species to another new magnetic species (g = 2.47, 2.26, and 1.91). This species is only seen in the presence of substrate, and its stability reflects the catalytic potency of the effector molecule. The EPR and UV-visible spectra of cytochrome P-420 depend upon the manner in which the P-420 is generated. Incubation with acetone or reaction with N-ethylmaleimide or diethyl pyrocarbonate generates P-420 with different spectral characteristics. Through identification of active-site amino acids by chemical modification and comparison with porphyrin model complexes, the range of ligands likely to participate in each of the EPR detectable species is assigned. Mechanisms of interconversion of these species and their bearing on catalysis are discussed.

MeSH Terms
Azides/pharmacology Cyanides/pharmacology Cytochrome P-450 Enzyme System/metabolism Electron Spin Resonance Spectroscopy Imidazoles/pharmacology Kinetics Ligands Protein Binding Protein Conformation Pseudomonas/metabolism Temperature
Chemicals
Azides Cyanides Imidazoles Ligands Cytochrome P-450 Enzyme System
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Lipscomb J D
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1980-07-22
Pages
3590-9
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · R01 GM024689 · United States
NIADDK NIH HHS · AM 00562 · United States
NIGMS NIH HHS · GM 21161 · United States
NIGMS NIH HHS · GM 24689 · United States
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